A Summarized Resource of NIH Guidelines for Research Involving
Recombinant DNA Molecules
Compliance with the NIH Guidelines for Research Involving Recombinant DNA ( http://osp.od.nih.gov/office-biotechnologyactivities/biosafety/nih-guidelines ) is mandatory for every institution that receives NIH funding for research involving recombinant
DNA (rDNA) or synthetic nucleic acids. It is the responsibility of each investigator to make sure that his/her laboratory is in compliance. If your experiments require registration, go to http://www.research.usf.edu/dric/biosafety/forms.asp
register. This outline is intended only to serve as a summarized resource to the NIH Guidelines . If you are unsure in which category your experiments fall, please contact us at biosafety@research.usf.edu
or via telephone at 974-0954
Section III-A & B & C – Experiments that require registration and NIHOBA and USF IBC approval Prior to initiation:
1.
Deliberate transfer of a drug resistance trait to microorganisms that are not known to acquire the trait naturally if such acquisition could compromise the use of the drug to control disease. (Section III-A-1-a)
2.
Cloning of toxin molecules with LD
50
of less than 100 ng / kilogram body weight. (Section III-B-1)
3.
Experiments that involve the deliberate transfer of recombinant DNA, or DNA or RNA derived from recombinant DNA, into one or more human research participant. (Section III-C-1)
Section III-D - Experiments that require registration & USF IBC approval Prior to initiation:
1.
Experiments using Risk Group 2, 3, or 4 agents as host-vector systems. (Section III-D-1)
2.
Experiments in which DNA from Risk Group 2, 3, or 4 agents is cloned into nonpathogenic prokaryotic or lower eukaryotic host-vector systems. (Section III-D-2-a)
3.
Experiments in which DNA from restricted agents is cloned into nonpathogenic prokaryotic or lower eukaryotic host-vector systems. (Section III-D-2-b)
4.
Experiments involving the use of infectious DNA or RNA viruses from Risk Group 2, 3 or 4 in tissue culture systems; or defective recombinant viruses in the presence of helper virus or packaging cells in tissue culture systems (this includes all eukaryotic viruses). (Section III-D-3)
5.
Experiments that generate transgenic animals, including insects. (Section III-D-4-b)
6.
Experiments involving viable rDNA-modified microorganisms tested on whole animals.(Section III-D-4-b)
7.
Experiments involving whole plants that require BSL3 or BSL4 containment. (Section III-D-5)
8.
Experiments involving more than 10 liters of culture.(Section III-D-6)
9.
Experiments involving human influenza strains H2N2, 1918 H1N1, and/or highly pathogenic H5N1.(Section III-D-7)
Section III-E - Experiments that require registration simultaneous with initiation :(USF Expedited review)
1.
Introduction into cultured cells of any rDNA containing greater than half but less than 2/3 of a eukaryotic viral genome (with the exception of Risk Group 3 or 4 agents). (Section III-E-1)
2.
Experiments involving whole plants that require BSL1 or BSL2 containment.(Section III-E-2)
3.
Cloning in non-pathogenic prokaryotes and non-pathogenic lower eukaryotes.(Section III-E)
4.
Experiments involving breeding of transgenic rodents that contain more than 50 percent of the genome of an exogenous eukaryotic virus from a single family, in order to prevent inadvertent reconstitution of an exogenous virus in the resultant transgenic rodent. (Section III-E-3)
5.
Experiments involving breeding of transgenic rodents in which the transgenic rodent's transgene is under the control of a gammaretroviral long terminal repeat (LTR), in order to address the small risk of recombination with endogenous retroviruses which could potentially result in mobilization of the transgene via a replication-competent mouse retrovirus.
(Section III-E-3,Appendix C-VIII (2))
6.
Cloning of all other DNA in E. coli K12, S. cerevisiae , and B. subtilis host-vector systems (with the exception of DNA from
Risk Group 3 or 4 pathogens). (Appendix C-II, C-III, C-IV)
Section III-F - Experiments that are exempt and do not require USF IBC registration :
1.
Use of rDNA that is not in organisms or viruses. (Section III-F-1)
2.
Purchase or transfer of transgenic rodents that may be maintained at BL1 containment.(Appendix C-VI)
3.
Introduction into cultured cells of any recombinant DNA containing less than half of a eukaryotic viral genome (with the exception of Risk Group 3 or 4 pathogens). (Appendix C-I)
4.
Breeding 2 different transgenic strains of rodents to generate novel transgenic strains requiring BL1 containment. (Appendix
C-VII)
RCDC#049.2
Revised 08/25/2015